Canonical Allele Identifier: CA389267017
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259235A>C , CM000676.2:g.24259235A>C GRCh38
NC_000014.8:g.24728441A>C , CM000676.1:g.24728441A>C GRCh37
NC_000014.7:g.23798281A>C NCBI36
NG_007150.1:g.8932T>G
NG_007150.2:g.8932T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.999T>G MANE Select ENSP00000206765.6:p.Asp333Glu
ENST00000206765.10:c.999T>G ENSP00000206765.6:p.Asp333Glu
ENST00000544573.5:c.-28-847T>G ENSP00000439446.1:n.-28-847T>G
ENST00000559136.1:c.72T>G ENSP00000453337.1:p.Asp24Glu
NM_000359.2:c.999T>G NP_000350.1:p.Asp333Glu
NM_000359.3:c.999T>G MANE Select NP_000350.1:p.Asp333Glu